Current through Register Vol. 30, No. 52, December 27, 2024
A.Before using an
automated dispensing system as defined in
R4-23-110, a pharmacy
permittee or pharmacist-in-charge of a provider pharmacy shall:
1. Notify the Board or its staff in writing
of the intent to use an automated dispensing system, including the name and
type of system;
2. Obtain a
separate controlled substances registration at the location of each long-term
care facility at which an automated dispensing system containing controlled
substances will be located as required by federal law; and
3. Maintain copies of the registrations
required under subsection (A)(2) at the provider pharmacy for inspection by the
Board or its staff.
B.A
pharmacy permittee or pharmacist-in-charge of a provider pharmacy shall ensure:
1. Drugs contained in an automated dispensing
system remain the property of the provider pharmacy,
2. Controlled substance drugs contained in an
automated dispensing system are included in all inventories required under
A.R.S. §36-2523(B) and
R4-23-1003(A),
3. Schedule II drugs are not stocked in an
automated dispensing system, and
4.
A separate emergency drug supply unit is available in the long-term care
facility to meet the requirements of
R4-23-701.02.
C.A pharmacy permittee or
pharmacist-in-charge of a provider pharmacy shall:
1. Ensure that policies and procedures as
required in subsection (D) for the use of an automated dispensing system in a
long-term care facility are prepared, implemented, and complied with;
2. Review biennially and, if necessary,
revise the policies and procedures required under subsection (D);
3. Document the review required under
subsection (C)(2);
4. Assemble the
policies and procedures as a written or electronic manual; and
5. Make the policies and procedures available
for employee reference and inspection by the Board or its staff within the
pharmacy and at any location outside of the pharmacy where the automated
dispensing system is used.
D.A pharmacy permittee or
pharmacist-in-charge of a provider pharmacy shall ensure the written policies
and procedures include:
1. Drug removal
procedures that include the following:
a. A
drug is provided only by a valid prescription order for an individual long-term
care facility resident;
b. A drug
is dispensed from an automated dispensing system only after a pharmacist has:
i. Reviewed and verified the resident's
prescription order as required by
R4-23-402(A),
and
ii. Electronically authorized
the access for that drug for that particular resident, and
c. The automated dispensing system labels
each individual drug packet with a resident specific label that complies with
R4-23-701.01(2) and contains the resident's room number or facility
identification number; and
2. Security procedures that include the
following:
a. The pharmacy permittee or
pharmacist-in-charge of the provider pharmacy is responsible for authorizing
user access, including adding and removing users and modifying user
access;
b. Each authorized user is
a licensee of the Board or authorized licensed personnel of the long-term care
facility; and
c. The automated
dispensing system is secured at the long-term care facility by electronic or
mechanical means or a combination thereof designed to prevent unauthorized
access;
3. Drug stocking
procedures that include the following:
a.
Automated dispensing systems that use non-removable containers that do not
allow prepackaging of the container as set out in subsection (D)(3)(b):
i. Are stocked at the long-term care facility
by an Arizona licensed pharmacist employed by the provider pharmacy, or by an
Arizona licensed intern, graduate intern, technician or technician trainee
under the direct onsite supervision of an Arizona licensed pharmacist;
and
ii. Utilize bar code or other
technologies to ensure the correct drug is placed in the correct canister or
container; and
b.
Automated dispensing systems that use removable containers may be stocked at
the long-term care facility by an authorized user provided:
i. The prepackaging of the container occurs
at the provider pharmacy;
ii. A
pharmacist verifies the container has been properly filled and labeled, and the
container is secured with a tamper-evident seal;
iii. The individual containers are
transported to the long-term care facility in a secure, tamperevident shipping
container; and
iv. The automated
dispensing system uses microchip, bar-coding, or other technologies to ensure
the containers are accurately loaded in the automated dispensing system;
and
4.
Recordkeeping and report procedures that include the following:
a. All events involving the access of the
automated dispensing system are recorded electronically and maintained for not
less than two years;
b. The
provider pharmacy is capable of producing a report of all transactions of the
automated dispensing system including:
i. A
single drug usage report that complies with
R4-23-408(B)(5);
and
ii. An authorized user history
including date and time of access and type of transaction; and
c. The provider pharmacy has
procedures to safeguard the storage, packaging, and distribution of drugs by
monitoring:
i. Current inventory;
ii. Expiration dates;
iii. Controlled substance
dispensing;
iv. Re-dispense
requests; and
v. Wastage.
E.A pharmacy
permittee or pharmacist-in-charge of a provider pharmacy shall:
1. Ensure that an electronic log is kept for
each container fill that includes:
a. An
identification of the container by drug name and strength, and container
number;
b. The drug's manufacturer
or National Drug Code (NDC) number;
c. The expiration date and lot number from
the manufacturer's stock bottle that is used to fill the container. If multiple
lot numbers of the same drug are added to a container, each lot number and
expiration date shall be documented;
d. The date the container is
filled;
e. Documentation of the
identity of the licensee who placed the drug into the container; and
f. If the licensee who filled the container
is not a pharmacist, documentation of the identity of the pharmacist who
supervised the non-pharmacist licensee; and
2. Maintain the electronic log for inspection
by the Board or its staff for not less than two years.
F.A pharmacy permittee or
pharmacist-in-charge of a provider pharmacy shall:
1. Implement an ongoing quality assurance
program that monitors performance of the automated dispensing system and
compliance with the established policies and procedures that includes:
a. Training in the use of the automated
dispensing system for all authorized users,
b. Maintenance and calibration of the
automated dispensing system as recommended by the device
manufacturer,
c. Routine accuracy
validation testing no less than every three months, and
d. Downtime and malfunction procedures to
ensure the timely provision of medication to the long-term care facility
resident, and
2.
Maintain documentation of the requirements of subsections (F)(1)(b) and
(F)(1)(c) for inspection by the Board or its staff for not less than two
years.
G.The Board may
prohibit a pharmacy permittee or pharmacist-in-charge from using an automated
dispensing system in a long-term care facility if the pharmacy permittee or the
pharmacy permittee's employees do not comply with the requirements of
subsections (A) through (F).